A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv804140



Internal ID15751410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:124540664..124546393hg38UCSC Ensembl
Innerchr12:125025210..125030939hg19UCSC Ensembl
Innerchr12:123591163..123596892hg18UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg385730
hg195730
hg185730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560584
Supporting Variants
Samples
Known GenesNCOR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv804140
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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